DERMAHAN UV SUN

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
DERMAHAN UV SUN
Generic name
ADENOSINE, NIACINAMIDE
Manufacturer
LAON COMMERCE co ltd
Product type
HUMAN OTC DRUG
SPL set ID
f992b41b-850b-37e1-e053-6294a90adb4b
SPL ID
f992b41b-850a-37e1-e053-6294a90adb4b
Version
1
Effective date
2023-04-17
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:52:30
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

1. If there are any abnormal symptoms or side effects such as red spots, swelling, or itching when using cosmetics or direct sunlight after use, consult a specialist. 2. Refrain from using it on injured areas, etc. 3. Precautions for storage and handling A) Keep it out of reach of children. B) Keep away from direct sunlight 3. Protects the skin from UV rays(SPF50+/PA++++) Helps whiten the skin. It helps to improve wrinkles on the skin.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.